Metalated aziridines for cross-coupling with aryl and alkenyl halides via palladium catalysis

Org Lett. 2010 Nov 19;12(22):5085-7. doi: 10.1021/ol101904a. Epub 2010 Oct 14.

Abstract

The palladium-catalyzed coupling of an aziridinylzinc chloride intermediate with alkenyl and aryl halides has been demonstrated. The method provides products with retention of aziridine stereochemistry. The utility of the coupling procedure is illustrated in the synthesis of structures related to l-furanomycin.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Alkenes / chemistry*
  • Amino Acids / chemical synthesis*
  • Amino Acids / chemistry
  • Aziridines / chemistry*
  • Catalysis
  • Chlorides / chemistry
  • Combinatorial Chemistry Techniques
  • Hydrocarbons, Halogenated / chemistry*
  • Molecular Structure
  • Palladium / chemistry*
  • Stereoisomerism
  • Zinc Compounds / chemistry

Substances

  • Alkenes
  • Amino Acids
  • Aziridines
  • Chlorides
  • Hydrocarbons, Halogenated
  • Zinc Compounds
  • furanomycin
  • Palladium
  • zinc chloride